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1-Octyn-3-ol, 7-methoxy-3,7-dimethyl-6-(phenylseleno)-, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76436-83-4

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76436-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76436-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,3 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76436-83:
(7*7)+(6*6)+(5*4)+(4*3)+(3*6)+(2*8)+(1*3)=154
154 % 10 = 4
So 76436-83-4 is a valid CAS Registry Number.

76436-83-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name acetic acid,7-methoxy-3,7-dimethyl-6-phenylselanyloct-1-yn-3-ol

1.2 Other means of identification

Product number -
Other names 1-ethynyl-5-methoxy-1,5-dimethyl-4-phenylselenenylhexyl acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:76436-83-4 SDS

76436-83-4Relevant academic research and scientific papers

A MECHANISM ON GENERATION AND RECYCLE OF THE SELENENYLATING REAGENTS IN ELECTROCHEMICAL OXYSELENENYLATION-DESELENENYLATION OF OLEFINS

Uneyama, Kenji,Ono, Michio,Torii, Sigeru

, p. 35 - 44 (2007/10/02)

The transformation of olefins 1 into allylic ethers and alcohols 2 (R = Me or H) was performed in 70-90percent yields, using a catalytic amount of diphenyl diselenide, by an electrochemical oxyselenenylation-deselenenylation sequence.The electrooxidation

A halide ion promoted electrochemical oxyselenenylation of olefins

Torii, Sigeru,Uneyama, Kenji,Ono, Michio

, p. 2741 - 2744 (2007/10/02)

A novel electrolytic transformation of olefins 1 into oxyselenides 2 has been performed in high yields and high regioselectivities by elctrolyzing olefins in protic solvents (MeOH, AcOH, H2O-MeCN) containing Et4NX (X = Cl, Br, I) and diphenyl diselenide using platinum foils.

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